Evidence map›Paper›PMID 32447348›Full record

Observational studyBone marrow transplantation2020

Cost and efficacy of peripheral stem cell mobilization strategies in multiple myeloma.

Zoé Van de Wyngaert, Virginie Nerich, Guillemette Fouquet, Marie-Lorraine Chrétien, Denis Caillot, Nabih Azar, Laurent Garderet, Pascal Lenain, Margaret Macro, Jean-Henri Bourhis and 18 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Bone marrow transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Autologous Stem Cell Collection after Daratumumab, Bortezomib, Thalidomide, and Dexamethasone versus Bortezomib, Cyclophosphamide, and Dexamethasone in Newly Diagnosed Multiple Myeloma.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2023
    Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 8 institutions in 1 country.

Zoé Van de Wyngaert *CHU Lille, Service des Maladies du Sang, F-59000, Lille, France.ORCID http://orcid.org/0000-0001-9463-2823
Virginie Nerich *Department of Pharmacy, University Hospital of Besançon, Univ. Bourgogne Franche-Comté, Besançon, France.
Guillemette FouquetInstitut Imagine, Inserm U1163, Hôpital Necker, APHP, Paris, France.
Marie-Lorraine ChrétienDepartment of Hematology, CHU, Dijon, France.
Denis CaillotDepartment of Hematology, CHU, Dijon, France.
Nabih AzarHôpital Pitié Salpêtrière, Service d'Hématologie, F-75013, Paris, France.
Laurent GarderetHématologie et thérapie cellulaire, Hôpital Saint Antoine, APHP, Université Paris-Sorbonne, INSERM UMRs 938, Paris, France.
Pascal LenainCentre Henri Becquerel, Rouen, France.
Margaret MacroInstitut d'hématologie, CHU, Caen, France.
Jean-Henri BourhisDepartment of Hématologie, Institut Gustave Roussy, Villejuif, France.
Ramdane BelhocineHématologie et thérapie cellulaire, Hôpital Saint Antoine, APHP, Université Paris-Sorbonne, INSERM UMRs 938, Paris, France.
Arnaud JaccardHématologie clinique et thérapie cellulaire, CHU, Limoges, France.
Lionel KarlinService d'Hématologie, Hospices Civils de Lyon, Lyon Sud, France.
Arthur BobinHematology and Inserm CIC 1402, CHU, Poitiers, France.
Niels MoyaHematology and Inserm CIC 1402, CHU, Poitiers, France.
Thomas SystchenkoHematology and Inserm CIC 1402, CHU, Poitiers, France.
Cecile GruchetHematology and Inserm CIC 1402, CHU, Poitiers, France.
Christine GiraudHematology and Inserm CIC 1402, CHU, Poitiers, France.
Stéphanie GuidezHematology and Inserm CIC 1402, CHU, Poitiers, France.
Claire DarrasHematology and Inserm CIC 1402, CHU, Poitiers, France.
Isabelle PrincetHematology and Inserm CIC 1402, CHU, Poitiers, France.
Cyrille TouzeauHematology Department, University Hospital Hotel-Dieu, Nantes, France.
Philippe MoreauHematology Department, University Hospital Hotel-Dieu, Nantes, France.
Cyrille HulinDepartment of Hematology, CHU, Bordeaux, France.
Erik DeconinckDepartment of Hematology, CHU, Besançon, France.ORCID http://orcid.org/0000-0002-6006-8088
Samuel Limat *Department of Pharmacy, University Hospital of Besançon, Univ. Bourgogne Franche-Comté, Besançon, France.
Xavier Leleu *Hematology and Inserm CIC 1402, CHU, Poitiers, France. xavier.leleu@chu-poitiers.fr.
IFM (Intergroupe Français du Myélome – IFM 2014-05)
Inserm · FRCentre Hospitalier Universitaire de Bordeaux · FRSorbonne Université · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Lille · FRCHU Dijon Bourgogne · FRHospices Civils de Lyon · FRInstitut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mobilization of peripheral blood stem cells (PBSC) can be performed using plerixafor, which is expensive, or high-dose cyclophosphamide (HDCy). We hypothesized that the overall cost of mobilization with plerixafor might not be greater if the cost of complication management was considered. We performed a cost analysis of these two strategies. This multicentric observational study recruited patients with myeloma who underwent a first PBSC mobilization. We considered direct medical costs, including hospitalization, mobilization agents, apheresis, and supportive treatments. We included 111 patients, 54 and 57 in the HDCy and plerixafor groups, respectively. Cost of mobilization with HDCy was 5097 ± 2982€ vs. 10958 ± 1789€ for plerixafor (p < 0.0001). Cost of agents used was 1287 ± 779€ vs. 6552 ± 509€, respectively (p = 0.0009). The mean number of days of hospitalization was 2 and 2.1 days, respectively (p = 0.035). All patients achieved the minimum PBSC collection target (p = 1.0); however, ASCT was performed with HDCy in 67% patients and with plerixafor in 86% (p = 0.02). Plerixafor mobilization incurred a greater cost, mostly due to the greater cost of the drug. Hospitalization length in the two groups was similar in our series. Interestingly, plerixafor appeared to be a very effective and safe mobilizing approach translating into a greater ASCT success.

Indexed as

Heterocyclic CompoundsMultiple MyelomaPeripheral Blood Stem CellsCyclophosphamideGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHumansCyclophosphamideGranulocyte Colony-Stimulating FactorHeterocyclic Compounds

Identifiers

PMID32447348
OpenAlexW3026184068

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.